Canonical Allele Identifier: CA693845741

Gene: CLECL1P

Linked Data

• dbSNP Id: rs1283705329
• gnomAD v3: 12-9723337-TATA-T
• gnomAD v4: 12-9723337-TATA-T
• MyVariant Identifiers: chr12:g.9875934_9875936del (hg19) ; chr12:g.9723338_9723340del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9723341_9723343del , CM000674.2:g.9723341_9723343del	GRCh38
NC_000012.11:g.9875937_9875939del , CM000674.1:g.9875937_9875939del	GRCh37
NC_000012.10:g.9767204_9767206del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000702603.1:n.150-527_150-525del
ENST00000327839.4:n.352-527_352-525del
ENST00000621400.5:n.263-527_263-525del
ENST00000327839.3:c.317-527_317-525del	ENSP00000331766.3:n.317-527_317-525del
ENST00000542530.5:c.172-527_172-525del
ENST00000621400.4:c.317-527_317-525del	ENSP00000483624.1:n.317-527_317-525del
NM_001253750.1:c.317-527_317-525del	NP_001240679.1:n.317-527_317-525del
NM_001267701.1:c.317-527_317-525del	NP_001254630.1:n.317-527_317-525del
NM_172004.3:c.317-527_317-525del	NP_742001.1:n.317-527_317-525del
XM_011520574.1:c.317-527_317-525del	XP_011518876.1:n.317-527_317-525del
XM_011520574.2:c.317-527_317-525del	XP_011518876.1:n.317-527_317-525del
XM_017018885.1:c.149-527_149-525del	XP_016874374.1:n.149-527_149-525del
NR_172485.1:n.349-527_349-525del
NR_172486.1:n.349-527_349-525del